A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149341



Internal ID15527930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84845680..84874775hg38UCSC Ensembl
Innerchr16:84879286..84908381hg19UCSC Ensembl
Innerchr16:83436787..83465882hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3829096
hg1929096
hg1829096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573470
Supporting Variants
SamplesHGDP00562
Known GenesCRISPLD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149341
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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